A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559680



Internal ID18857961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78026370..78064108hg38UCSC Ensembl
Innerchr16:78060267..78098005hg19UCSC Ensembl
Innerchr16:76617768..76655506hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3837739
hg1937739
hg1837739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058985
Supporting Variants
Samples
Known GenesCLEC3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559680
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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